Broad-spectrum monoclonal antibodies against chikungunya virus E1 structural protein

ABSTRACT

The present invention provides a new antibody against ECSA type Chikungunya virus, WA type Chikungunya virus, and Asian type Chikungunya virus or an antigen-binding fragment of the antibody. The antibody against Chikungunya virus or the antigen-binding fragment of the antibody of the present invention includes a heavy chain variable region or a heavy chain (1), (2), or (3) and a light chain variable region or a light chain (4).

TECHNICAL FIELD

The present invention relates to a new antibody against Chikungunya virus or an antigen-binding fragment of the antibody, and use of the same.

BACKGROUND ART

In Southeast Asia and elsewhere, epidemic diseases are transmitted by mosquitoes such as Aedes aegypti and Aedes albopictus. The epidemic diseases include dengue fever, Chikungunya fever, and Zika fever.

If the epidemic disease is suspected, it is necessary to determine which epidemic disease the patient has prior to treatment. For this reason, the causative virus test is performed.

SUMMARY OF INVENTION Technical Problem

The inventors of the present invention have obtained CK47 antibody and CK119 antibody that bind to an E1 protein that constitutes the envelope sugar protein (hereinafter, also referred to as “Env protein”) of Chikungunya virus (hereinafter, also referred to as “CHIKV”) which is the pathogen of Chikungunya fever. However, CK47 antibody was bound strongly only to one genotype (ECSA) of three genotypes (ECSA (East/Central/South African), WA (West African), and Asian) of CHIKV. Furthermore, while CK119 antibody was bound to the three genotypes of CHIKV, it is strongly cross-reactive to Sindbis virus (SINV) of the same Alphavirus genus. Thus, there is a need for an antibody that binds to the three genotypes of CHIKV and does not bind to SINV.

With the foregoing in mind, it is an object of the present invention to provide a new antibody against three genotypes of CHIKV, namely ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV or an antigen-binding fragment of the antibody.

Solution to Problem

In order to achieve the above object, the present invention provides an antibody against Chikungunya virus or an antigen-binding fragment of the antibody (hereinafter, also referred to as “antibody or the like”), including the following heavy chain variable region (1), (2), or (3) and the following light chain variable region (4).

(1) a heavy chain variable region including heavy chain complementarity determining regions (CDRH)1, CDRH2, and CDRH3:

CDRH1 is a polypeptide including the following amino acid sequence (H1-A),

CDRH2 is a polypeptide including the following amino acid sequence (H2-A), and

CDRH3 is a polypeptide including the following amino acid sequence (H3-A), wherein

(H1-A) the following amino acid sequence (H1-A1), (H1-A2), or (H1-A3):

(H1-A1) an amino acid sequence of SEQ ID NO: 1 (GYTFTSYW),

(H1-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 1, and

(H1-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 1,

(H2-A) the following amino acid sequence (H2-A1), (H2-A2), or (H2-A3):

(H2-A1) an amino acid sequence of SEQ ID NO: 2 (IYPGDGDTRYT),

(H2-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 2, and

(H2-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 2,

(H3-A) the following amino acid sequence (H3-A1), (H3-A2), or (H3-A3):

(H3-A1) an amino acid sequence of SEQ ID NO: 3 (SYDPFDY),

(H3-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 3, and

(H3-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 3.

(2) a heavy chain variable region including CDRH1, CDRH2, and CDRH3:

CDRH1 is a polypeptide including the following amino acid sequence (H1-B),

CDRH2 is a polypeptide including the following amino acid sequence (H2-B), and

CDRH3 is a polypeptide including the following amino acid sequence (H3-B), wherein

(H1-B) the following amino acid sequence (H1-B1), (H1-B2), or (H1-B3):

(H1-B1) an amino acid sequence of SEQ ID NO: 4 (GYAFSTSW),

(H1-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 4, and

(H1-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 4,

(H2-B) the following amino acid sequence (H2-B1), (H2-B2), or (H2-B3):

(H2-B1) an amino acid sequence of SEQ ID NO: 5 (IYPGDGDT),

(H2-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 5, and

(H2-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 5,

(H3-B) the following amino acid sequence (H3-B1), (H3-B2), or (H3-B3):

(H3-B1) an amino acid sequence of SEQ ID NO: 6 (SNDGYYVGY),

(H3-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 6, and

(H3-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 6.

(3) a heavy chain variable region including CDRH1, CDRH2, and CDRH3:

CDRH1 is a polypeptide including the following amino acid sequence (H1-C),

CDRH2 is a polypeptide including the following amino acid sequence (H2-C),

CDRH3 is a polypeptide including the following amino acid sequence (H3-C), wherein

(H1-C) the following amino acid sequence (H1-C1), (H1-C2), or (H1-C3):

(H1-C1) an amino acid sequence of SEQ ID NO: 7 (GYTFTSYY),

(H1-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 7, and

(H1-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 7,

(H2-C) the following amino acid sequence (H2-C1), (H2-C2), or (H2-C3):

(H2-C1) an amino acid sequence of SEQ ID NO: 8 (INPSNGGT),

(H2-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 8, and

(H2-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 8,

(H3-C) the following amino acid sequence (H3-C1), (H3-C2), or (H3-C3):

(H3-C1) an amino acid sequence of SEQ ID NO: 9 (GYYGNPFFAY),

(H3-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 9, and

(H3-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 9.

(4) a light chain variable region including light chain complementarity determining regions (CDRL)1, CDRL2, and CDRL3:

CDRL1 is a polypeptide including the following amino acid sequence (L1-A),

CDRL2 is a polypeptide including the following amino acid sequence (L2-A),

CDRL3 is a polypeptide including the following amino acid sequence (L3-A), wherein

(L1-A) the following amino acid sequence (L1-A1), (L1-A2), or (L1-A3):

(L1-A1) an amino acid sequence of SEQ ID NO: 10 (ENVVTY),

(L1-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 10, and

(L1-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 10,

(L2-A) the following amino acid sequence (L2-A1), (L2-A2), or (L2-A3):

(L2-A1) an amino acid sequence of SEQ ID NO: 11 (GAS),

(L2-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 11, and

(L2-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 11,

(L3-A) the following amino acid sequence (L3-A1), (L3-A2), or (L3-A3):

(L3-A1) an amino acid sequence of SEQ ID NO: 12 (GQGYSYPYT),

(L3-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 12, and

(L3-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 12.

The present invention also provides an antibody against Chikungunya virus or an antigen-binding fragment of the antibody, including the following heavy chain variable region (1), (2), or (3) and the following light chain variable region (4).

(1) a heavy chain variable region including a polypeptide consisting of the following amino acid sequence (H-A):

(H-A) the following amino acid sequence (H-A1), (H-A2), or (H-A3):

(H-A1) an amino acid sequence of SEQ ID NO: 13,

(H-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 13, and

(H-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 13.

(2) a heavy chain variable region including a polypeptide consisting of the following amino acid sequence (H-B):

(H-B) the following amino acid sequence (H-B1), (H-B2), or (H-B3):

(H-B1) an amino acid sequence of SEQ ID NO: 14,

(H-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 14, and

(H-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 14.

(3) a heavy chain variable region including a polypeptide consisting of the following amino acid sequence (H-C):

(H-C) the following amino acid sequence (H-C1), (H-C2), or (H-C3):

(H-C1) an amino acid sequence of SEQ ID NO: 15,

(H-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 15, and

(H-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 15.

(4) a light chain variable region including a polypeptide consisting of the following amino acid sequence (L-A):

(L-A) the following amino acid sequence (L-A1), (L-A2), or (L-A3):

(L-A1) an amino acid sequence of SEQ ID NO: 16,

(L-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 16, and

(L-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 16.

The present invention also provides an antibody against Chikungunya virus or an antigen-binding fragment of the antibody, including the following heavy chain (1), (2), or (3) and the following light chain (4).

(1) a heavy chain including a polypeptide consisting of the following amino acid sequence (HA):

(HA) the following amino acid sequence (HA1), (HA2), or (HA3):

(HA1) an amino acid sequence of SEQ ID NO: 17,

(HA2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 17, and

(HA3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 17.

(2) a heavy chain including a polypeptide consisting of the following amino acid sequence (HB):

(HB) the following amino acid sequence (HB1), (HB2), or (HB3):

(HB1) an amino acid sequence of SEQ ID NO: 18,

(HB2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 18, and

(HB3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 18.

(3) a heavy chain including a polypeptide consisting of the following amino acid sequence (HC):

(HC) the following amino acid sequence (HC1), (HC2), or (HC3):

(HC1) an amino acid sequence of SEQ ID NO: 19,

(HC2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 19, and

(HC3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 19.

(4) a light chain including a polypeptide consisting of the following amino acid sequence (LA):

(LA) the following amino acid sequence (LA1), (LA2), or (LA3):

(LA1) an amino acid sequence of SEQ ID NO: 20,

(LA2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 20, and

(LA3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 20.

The present invention also provides a detection kit for Chikungunya virus (hereinafter, also referred to as a “detection kit”), including: the antibody or the antigen-binding fragment of the antibody of the present invention.

The present invention also provides a method for detecting Chikungunya virus (hereinafter, also referred to as a “detection method”), including: a detection step of bringing a sample into contact with the antibody or the antigen-binding fragment of the antibody of the present invention to bind Chikungunya virus in the sample to the antibody or the antigen-binding fragment of the antibody, thereby detecting Chikungunya virus in the sample.

Advantageous Effects of Invention

According to the present invention, a new antibody that binds to three genotypes of CHIKV, namely ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV can be provided. Thus, according to the antibody or the like of the present invention, for example, CHIKV can be detected regardless of the genotype, and therefore, it can be suitably used for a detection kit for CHIKV.

BRIEF DESCRIPTION OF DRAWINGS

FIGS. 1A to 1C show photographs showing the staining results of cells expressing the envelope protein in Example 2.

FIGS. 2A to 2D show photographs showing the staining results of SINV-infected cells in Example 3.

DESCRIPTION OF EMBODIMENTS Antibody or Antigen-Binding Fragment of the Antibody

As described above, the antibody against Chikungunya virus or the antigen-binding fragment of the antibody of the present invention includes the heavy chain variable region or heavy chain (1), (2), or (3) and the light chain variable region or light chain (4). The antibody or the like of the present invention is characterized in that it includes the heavy chain variable region or the heavy chain (1), (2), or (3) and the light chain variable region or the light chain (4), and other configurations and conditions are not particularly limited. The antibody or the like of the present invention binds to ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV.

The antibody or the like of the present invention does not bind to, for example, Sindbis virus. Therefore, the antibody or the like of the present invention can be suitably used, for example, in a detection kit or the like for CHIKV to be described below.

In the present invention, “Chikungunya virus” refers to Chikungunya virus belonging to the genus Alphavirus of the family Togaviridae.

In the present invention, “Sindbis virus” refers to Sindbis virus belonging to the genus Alphavirus of the family Togaviridae.

The antibody or the like of the present invention binds to ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV as described above. The ECSA type CHIKV, the WA type CHIKV, and the Asian type CHIKV can be classified with reference to the Reference 1 below, for example. More specifically, the antibody or the like of the present invention binds to an Env protein of ECSA type CHIKV, an Env protein of WA type CHIKV, and an Env protein of Asian type CHIKV, for example. The Env protein refers to an envelope protein of CHIKV, for example. The Env protein is also referred to as a E3-E2-6K-E1 protein because it is composed of a 6K-E1 protein, an E2 protein, and an E3 protein, for example. The amino acid sequence of the Env protein of CHIKV can be referred to, for example, information registered in an existing data base. As a specific example, an Env protein derived from ECSA type CHIKV includes, for example, the following amino acid sequence (SEQ ID NO: 21) from positions 268 to 1247 in the amino acid sequence registered under the NCBI Accession NO.: BAP74220.1. An Env protein derived from WA type CHIKV includes, for example, the following amino acid sequence (SEQ ID NO: 22) from positions 268 to 1247 in the amino acid sequence registered under the NCBI Accession NO.: AAU43881.1. An Env protein derived from Asian type CHIKV includes, for example, the following amino acid sequence (SEQ ID NO: 23) from positions 268 to 1247 in the amino acid sequence registered under the NCBI Accession NO.: ADG95938.1.

Reference 1: Aekkachai Tuekprakhon et. al., “Variation at position 350 in the Chikungunya virus 6K-E1 protein determines the sensitivity of detection in a rapid E1-antigen test”, Scientific Report, vol. 8, Article Number:1094, 2018

Env protein derived from ECSA type CHIKV (SEQ ID NO: 21) MCLLANTTFPCSQPPCTPCCYEKEPEETLRMLEDNVMRPGYYQLLQASL TCSPHRQRRSTKDNFNVYKATRPYLAHCPDCGEGHSCHSPVALERIRNE ATDGTLKIQVSLQIGIKTDDSHDWTKLRYMDNHMPADAERAGLFVRTSA PCTITGTMGHFILARCPKGETLTVGFTDSRKISHSCTHPFHHDPPVIGR EKFHSRPQHGKELPCSTYVQSTAATTEEIEVHMPPDTPDRTLMSQQSGN VKITVNGQTVRYKCNCGGSNEGLTTTDKVINNCKVDQCHAAVTNHKKWQ YNSPLVPRNAELGDRQGKIHIPFPLANVTCRVPKARNPTVTYGKNQVIM LLYPDHPTLLSYRNMGEEPNYQEEWVMHKKEVVLTVPTEGLEVTWGNNE PYKYWPQLSTNGTAHGHPHEIILYYYELYPTMTVVVVSVATFILLSMVG MAAGMCMCARRRCITPYELTPGATVPFLLSLICCIRTAKAATYQEAAIY LWNEQQPLFWLQALIPLAALIVLCNCLRLLPCCCKTLAFLAVMSVGAHT VSAYEHVTVIPNTVGVPYKTLVNRPGYSPMVLEMELLSVTLEPTLSLDY ITCEYKTVIPSPYVKCCGTAECKDKNLPDYSCKVFTGVYPFMWGGAYCF CDAENTQLSEAHVEKSESCKTEFASAYRAHTASASAKLRVLYQGNNITV TAYANGDHAVTVKDAKFIVGPMSSAWTPFDNKIVVYKGDVYNMDYPPFG AGRPGQFGDIQSRTPESKDVYANTQLVLQRPAVGTVHVPYSQAPSGFKY WLKERGASLQHTAPFGCQIATNPVRAVNCAVGNMPISIDIPEAAFTRVV DAPSLTDMSCEVPACTHSSDFGGVAIIKYAASKKGKCAVHSMTNAVTIR EAEIEVEGNSQLQISFSTALASAEFRVQVCSTQVHCAAECHPPKDHIVN YPASHTTLGVQDISATAMSWVQKITGGVGLVVAVAALILIVVLCVSFSR H Env protein derived from WA type CHIKV (SEQ ID NO: 22) LCLLANTTFPCSQPPCTPCCYEKEPESTLRMLEDNVMRPGYYQLLKASL TCSPHRQRRSTKDNFNVYKATRPYLAHCPDCGEGHSCHSPIALERIRNE ATDGTLKIQVSLQIGIKTDDSHDWTKLRYMDSHTPADAERAGLLVRTSA PCTITGTMGHFILARCPKGETLTVGFTDSRKISHTCTHPFHHEPPVIGR ERFHSRPQHGKELPCSTYVQSTAATAEEIEVHMPPDTPDRTLMTQQSGN VKITVNGQTVRYKCNCGGSNEGLTTTDKVINNCKIDQCHAAVTNHKNWQ YNSPLVPRNAELGDRKGKIHIPFPLANVTCRVPKARNPTVTYGKNQVTM LLYPDHPTLLSYRNMGQEPNYHEEWVTHKKEVTLTVPTEGLEVTWGNNE PYKYWPQMSTNGTAHGHPHEIILYYYELYPTMTVVIVSVASFVLLSMVG TAVGMCVCARRRCITPYELTPGATVPFLLSLLCCVRTTKAATYYEAAAY LWNEQQPLFWLQALIPLAALIVLCNCLKLLPCCCKTLAFLAVMSIGAHT VSAYEHVTVIPNTVGVPYKTLVNRPGYSPMVLEMELQSVTLEPTLSLDY ITCEYKTVIPSPYVKCCGTAECKDKSLPDYSCKVFTGVYPFMWGGAYCF CDAENTQLSEAHVEKSESCKTEFASAYRAHTASASAKLRVLYQGNNITV AAYANGDHAVTVKDAKFVVGPMSSAWTPFDNKIVVYKGDVYNMDYPPFG AGRPGQFGDIQSRTPESKDVYANTQLVLQRPAAGTVHVPYSQAPSGFKY WLKERGASLQHTAPFGCQIATNPVRAVNCAVGNIPISIDIPDAAFTRVV DAPSVTDMSCEVPACTHSSDFGGVAIIKYTASKKGKCAVHSMTNAVTIR EADVEVEGNSQLQISFSTALASAEFRVQVCSTQVHCAAACHPPKDHIVN YPASHTTLGVQDISTTAMSWVQKITGGVGLIVAVAALILIVVLCVSFSR H Env protein from Asian type CHIKV (SEQ ID NO: 23) MCLLANTTFPCSQPPCTPCCYEKEPEKTLRMLEDNVMSPGYYQLLQASL TCSPRRQRRSIKDNFNVYKATRPYLAHCPDCGEGHSCHSPVALERIRNE ATDGTLKIQVSLQIGIKTDDSHDWTKLRYMDNHMPADAERAGLFVRTSA PCTITGTMGHFILARCPKGETLTVGFTDGRKISHSCTHPFHHDPPVIGR EKFHSRPQHGRELPCSTYAQSTAATAEEIEVHMPPDTPDRTLMSQQSGN VKITVNSQTVRYKCNCGDSNEGLTTTDKVINNCKVDQCHAAVTNHKKWQ YNSPLVPRNAELGDRKGKVHIPFPLANVTCRVPKARNPTVTYGKNQVIM LLYPDHPTLLSYRNMGEEPNYQEEWVTHKKEIRLTVPTEGLEVTWGNNE PYKYWPQLSTNGTAHGHPHEIILYYYELYPTMTVVVVSVASFVLLSMVG VAVGMCMCARRRCITPYELTPGATVPFLLSLICCIRTAKAATYQEAAVY LWNEQQPLFWLQALIPLAALIVLCNCLRLLPCCCKTLTFLAVLSVGAHT VSAYEHVTVIPNTVGVPYKTLVNRPGYSPMVLEMELLSVTLEPTLSLDY ITCEYKTVIPSPYVKCCGTAECKDKSLPDYSCKVFTGVYPFMWGGAYCF CDTENTQLSEAHVEKSESCKTEFASAYRAHTASASAKLRVLYQGNNVTV SAYANGDHAVTVKDAKFIVGPMSSAWTPFDNKIVVYKGDVYNMDYPPFG AGRPGQFGDIQSRTPESEDVYANTQLVLQRPSAGTVHVPYSQAPSGFKY WLKERGASLQHTAPFGCQIATNPVRAIVINCAVGNMPISIDIPDAAFTR VVDAPSLTDMSCEVSACTHSSDFGGVAIIKYAASKKGKCAVHSMTNAVT IREAEIEVEGNSQLQISFSTALASAEFRVQVCSTQVHCAAECHPPKDHI VNYPASHTTLGVQDISATAMSWVQKITGGVGLVVAVAALILIVVLCVSF SRH

The antibody or the like of the present invention includes, for example, an antibody that binds to a peptide fragment of the Env protein, in addition to an antibody that binds to CHIKV, more specifically, a protein consisting of the full-length amino acid sequence of the Env protein. The Env protein includes, for example, a mutant Env protein (E350D) in which the amino acid (glutamic acid (E) underlined in SEQ ID NO: 21) corresponding to the amino acid at position 826 (position 284 of the E1 protein and position 350 of 6K-E1 protein) in the amino acid sequence of SEQ ID NO: 21 is substituted with an aspartic acid (D). The Env protein includes, for example, a mutant Env protein (D350E) in which the amino acid (aspartic acid (D) underlined in SEQ ID NO: 22 or 23) corresponding to the amino acid at position 826 (position 284 of the E1 protein and position 350 of 6K-E1 protein) in the amino acid sequence of SEQ ID NO: 22 or 23 is substituted with a glutamic acid (E). Hereinafter, for example, the Env protein includes, in addition to an Env protein consisting of the full-length amino acid sequence, a mutant Env protein (E350D), and a mutant Env protein (D350E), the meaning of the peptide fragments of these Env proteins, unless otherwise indicated. The CK47 antibody particularly weakly binds to the mutant Env protein (E350D), the Env protein derived from WA type CHIKV, and Env protein derived from Asian type CHIKV. According to the antibody or the like of the present invention, for example, the mutant Env protein (E350D), the Env protein derived from WA type CHIKV, and the Env protein derived from Asian type CHIKV can also be detected.

The present invention may be, for example, a so-called “antibody” in which the molecular structure is an immunoglobulin, or an antigen-binding fragment of the antibody. The antibody or the like of the present invention may have the heavy chain variable region and the light chain variable region. When the present invention is an antibody, for example, its immunoglobulin class and isotype are not particularly limited. Examples of the immunoglobulin class include IgG, IgM, IgA, IgD, and IgE. Examples of the IgG include IgG1, IgG2, IgG3, and IgG4.

Examples of the antibody include monoclonal antibodies, polyclonal antibodies, recombinant antibodies, human (e.g., fully human) antibodies, humanized antibodies, chimeric antibodies, and multispecific antibodies.

The “antigen-binding fragment” in the present invention refers to a part of the antibody, e.g., a partial fragment which recognizes (binds to) the Chikungunya virus. Examples of the antigen-binding fragment include Fab, Fab′, F(ab′)₂, variable region fragments (Fv), disulfide bond Fv, single-chain Fv (scFv), bispecific antibodies, and polymers thereof.

The antibody or the like of the present invention may have, for example, a constant region in addition to the heavy chain variable region and the light chain variable region described above, and the constant region is, for example, a human constant region or a mouse constant region. In the case of the antibody (immunoglobulin), the constant region of a heavy chain includes regions CH1, CH2, and CH3, for example, and the constant region of a light chain includes a region CL, for example. When the antibody or the like of the present invention includes the constant region, for example, the heavy chain variable region is bound to at least one of CH1, CH2, and CH3, the light chain variable region is bound to the CL, and the heavy chain variable region is directly bound to the CH1, for example.

Generally, the heavy chain and the light chain of an antibody molecule each include three complementarity determining regions (CDRs). The CDR is also referred to as a hypervariable domain. The CDR is a region in which the primary structure is highly variable among the variable regions of the heavy chain and the light chain, and is usually separated in three sites on the primary structure. In the present invention, three sites of CDR in the heavy chain are denoted as heavy chain CDR1 (CDRH1), heavy chain CDR2 (CDRH2), and heavy chain CDR3 (CDRH3) from the amino terminal side in the amino acid sequence of the heavy chain, and three sites of CDR in the light chain are denoted as light chain CDR1 (CDRL1), light chain CDR2 (CDRL2), and light chain CDR3 (CDRL3) from the amino terminal side in the amino acid sequence of the light chain. These sites are conformationally close to each other and determine the specificity for the antigen to be bound.

Hereinafter, as to the antibody or the like of the present invention, the combination of the heavy chain variable region or heavy chain and the light chain variable region or light chain will be described. Regarding the description of the heavy chain variable region in each combination and the description of the heavy chain in each combination, reference can be made to one another. Regarding the description of the light chain variable region in each combination and description of the light chain in each combination, reference can be made to one another.

In the antibody or the like of the present invention, the combination of the heavy chain variable region or the heavy chain and the light chain variable region or the light chain is the combination of (1) and (4), the combination of (2) and (4), or the combination of (3) and (4).

Combination of (1) and (4)

The antibody or the like of the combination of (1) and (4) is also referred to as an antibody 3D11 group, for example. In the combination of (1) and (4), the heavy chain variable region (1) includes heavy chain complementarity determining regions (CDRH)1, CDRH2, and CDRH3, wherein CDRH1 is a polypeptide including the following amino acid sequence (H1-A), CDRH2 is a polypeptide including the following amino acid sequence (H2-A), and CDRH3 is a polypeptide including the following amino acid sequence (H3-A). Further, the light chain variable region (4) includes a light chain complementarity determining region (CDRL) 1, CDRL2, and CDRL3, wherein CDRL1 is a polypeptide including the following amino acid sequence (L1-A), CDRL2 is a polypeptide including the following amino acid sequence (L2-A), and CDRL3 is a polypeptide including the following amino acid sequence (L3-A).

(H1-A) the following amino acid sequence (H1-A1), (H1-A2), or (H1-A3):

(H1-A1) an amino acid sequence of SEQ ID NO: 1 (GYTFTSYW),

(H1-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 1, and

(H1-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, and inserted and/or added in the amino acid sequence of SEQ ID NO: 1.

(H2-A) the following amino acid sequence (H2-A1), (H2-A2), or (H2-A3):

(H2-A1) an amino acid sequence of SEQ ID NO: 2 (IYPGDGDTRYT),

(H2-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 2, and

(H2-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 2.

(H3-A) the following amino acid sequence (H3-A1), (H3-A2), or (H3-A3):

(H3-A1) an amino acid sequence of SEQ ID NO: 3 (SYDPFDY),

(H3-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 3, and

(H3-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 3.

(L1-A) the following amino acid sequence (L1-A1), (L1-A2), or (L1-A3):

(L1-A1) an amino acid sequence of SEQ ID NO: 10 (ENVVTY),

(L1-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 10, and

(L1-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 10.

(L2-A) the following amino acid sequence (L2-A1), (L2-A2), or (L2-A3):

(L2-A1) an amino acid sequence of SEQ ID NO: 11 (GAS),

(L2-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 11, and

(L2-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 11.

(L3-A) the following amino acid sequence (L3-A1), (L3-A2), or (L3-A3):

(L3-A1) an amino acid sequence of SEQ ID NO: 12 (GQGYSYPYT),

(L3-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 12, and

(L3-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 12.

In each CDR, the “identity” is, for example, a degree of identity when the sequences to be compared are appropriately aligned, and means a rate of occurrence (%) of an accurate match of amino acids between the sequences. The “identity” is 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more. The identity can be calculated, for example, by default parameters using analysis software such as BLAST, FASTA, and the like (hereinafter, the same applies).

In each CDR, “one or several” relating to substitution or the like is, for example, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1.

The substitution of the amino acid may be, for example, a conservative substitution (hereinafter, the same applies). The conservative substitution means substituting one or several amino acids with other amino acids and/or amino acid derivatives so as not to substantially alter the function of the protein. It is preferable that the properties and/or functions of “an amino acid that substitutes an amino acid” and “an amino acid to be substituted with an amino acid” be similar to each other, for example. Specifically, it is preferable that, for example, a hydrophobic and hydrophilic indicator (hydropathy), a chemical property such as polarity or charge, or a physical property such as a secondary structure of “an amino acid that substitutes an amino acid” and “an amino acid to be substituted with an amino acid” be similar to each other. Amino acids or amino acid derivatives having similar properties and/or functions are known in the art, for example. Specific examples of the nonpolar amino acid (hydrophobic amino acid) include alanine, valine, isoleucine, leucine, proline, tryptophan, phenylalanine, and methionine. Specific examples of the polar amino acid (neutral amino acid) include glycine, serine, threonine, tyrosine, glutamine, asparagine, and cysteine. Specific examples of the amino acid (basic amino acid) having a positive charge include arginine, histidine, and lysine. Specific examples of the amino acid (acidic amino acid) having a negative charge include an aspartic acid and a glutamic acid.

In the combination of (1) and (4), the heavy chain variable region (1) includes a polypeptide consisting of the following amino acid sequence (H-A), for example. Further, the light chain variable region (4) includes a polypeptide consisting of the following amino acid sequence (L-A), for example.

(H-A) the following amino acid sequence (H-A1), (H-A2), or (H-A3):

(H-A1) an amino acid sequence of SEQ ID NO: 13,

SEQ ID NO: 3: QVQLQQSGAELARPGASVKLSCKASGYTFTSYWMQWVKQRPGQGLEWIG AIYPGDGDTRYTQKFKGKATLTADKSSSTAYMQLSSLASEDSAVYYCAR SYDPFDYWGQGTTLTVSS, (H-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 13, and (H-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 13.

(L-A) the following amino acid sequence (L-A1), (L-A2), or (L-A3):

(L-A1) an amino acid sequence of SEQ ID NO: 16,

SEQ ID NO: 16: NIVMTQSPKSMSMSVGERVTLTCKASENVVTYVSWYQQKPEQSPKLLIY GASNRYTGVPDRFTGSGSATDFTLTISSVQAEDLADYHCGQGYSYPYTF GGGTKLEI, (L-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 16, and (L-A3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 16.

The amino acid sequence (H-A1) is a sequence including the amino acid sequences (H1-A1) of CDRH1, (H2-A1) of CDRH2, and (H3-A1) of CDRH3, for example. The amino acid sequence (H-A2) may be an amino acid sequence including the amino acid sequences (H1-A1) of CDRH1, (H2-A1) of CDRH2, and (H3-A1) of CDRH3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 13, for example. The amino acid sequence (H-A3) may be an amino acid sequence including the amino acid sequences (H1-A1) of CDRH1, (H2-A1) of CDRH, and (H3-A1) of CDRH3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 13, for example.

The amino acid sequence (L-A1) is a sequence including the amino acid sequences (L1-A1) of CDRL1, (L2-A1) of CDRL2, and (L3-A1) of CDRL3, for example. The amino acid sequence (L-A2) may be an amino acid sequence including the amino acid sequences (L1-A1) of CDRL1, (L2-A1) of CDRL2, and (L3-A1) of CDRL3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 16, for example. The amino acid sequence (L-A3) may be an amino acid sequence including the amino acid sequences (L1-A1) of CDRL1, (L2-A1) of CDRL2, and (L3-A1) of CDRL3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 16, for example.

In the antibody of the present invention, for example, the heavy chain variable region is the (H-A1) and the light chain variable region is the (L-A1). The antibody of this combination is hereinafter also referred to as an “antibody 3D11”.

In the polypeptide of the heavy chain variable region and the polypeptide of the light chain variable region, the “identity” is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more, respectively.

In the polypeptide of the heavy chain variable region and the polypeptide of the light chain variable region, “one or several” relating to substitution or the like is, for example, 1 to 20, 1 to 15, 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1, respectively.

In the combination of (1) and (4), the heavy chain (1) includes a polypeptide consisting of the following amino acid sequence (HA), for example. Further, the light chain (4) includes a polypeptide consisting of the following amino acid sequence (LA), for example.

(1) a heavy chain including a polypeptide consisting of the following amino acid sequence (HA):

(HA) the following amino acid sequence (HA1), (HA2), or (HA3):

(HA1) an amino acid sequence of SEQ ID NO: 17,

(HA2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 17, and

(HA3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 17.

(4) a light chain including a polypeptide consisting of the following amino acid sequence (LA):

(LA) the following amino acid sequence (LA1), (LA2), or (LA3):

(LA1) an amino acid sequence of SEQ ID NO: 20,

(LA2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 20, and

(LA3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 20.

The amino acid sequence (HA1) is a sequence including the amino acid sequences (H1-A1) of CDRH1, (H2-A1) of CDRH2, and (H3-A1) of CDRH3, and/or a sequence including the amino acid sequence (H-A1). The amino acid sequence (HA2) may be an amino acid sequence including the amino acid sequences (H1-A1) of CDRH1, (H2-A1) of CDRH2, and (H3-A1) of CDRH3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 17, for example. The amino acid sequence (HA2) may be an amino acid sequence including the amino acid sequence (H-A1) and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 17, for example. The amino acid sequence (HA3) may be an amino acid sequence including the amino acid sequences (H1-A1) of CDRH1, (H2-A1) of CDRH2, and (H3-A1) of CDRH3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 17, for example. The amino acid sequence (HA3) may be an amino acid sequence including the amino acid sequence (H-A1) and in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 17, for example.

The amino acid sequence (LA1) is a sequence including the amino acid sequences (L1-A1) of CDRL1, (L2-A1) of CDRL2, and (L3-A1) of CDRL3, and/or a sequence including the amino acid sequence (L-A1). The amino acid sequence (LA2) may be an amino acid sequence including the amino acid sequences (L1-A1) of CDRL1, (L2-A1) of CDRL2, and (L3-A1) of CDRL3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 20, for example. The amino acid sequence (LA2) may be an amino acid sequence including the amino acid sequence (L-A1) and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 20, for example. The amino acid sequence (LA3) may be an amino acid sequence including the amino acid sequences (L1-A1) of CDRL1, (L2-A1) of CDRL2, and (L3-A1) of CDRL3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 20, for example. The amino acid sequence (LA3) may be an amino acid sequence including the amino acid sequence (L-A1) and in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 20, for example.

In the antibody of the present invention, for example, the heavy chain is the (HA1) and the light chain is the (LA1). The antibody of this combination is hereinafter also referred to as “3D11”.

In the polypeptide of the heavy chain and the polypeptide of the light chain, the “identity” is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more, respectively.

In the polypeptide of the heavy chain and the polypeptide of the light chain, “one or several” relating to substitution or the like is, for example, 1 to 80, 1 to 60, 1 to 40, 1 to 30, 1 to 20, 1 to 15, 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1, respectively.

Combination of (2) and (4)

The antibody or the like of the combination of (2) and (4) is also referred to as, for example, an antibody 13H11 group. In the combination of (2) and (4), the heavy chain variable region (2) includes CDRH1, CDRH2, and CDRH3, wherein CDRH1 is a polypeptide including the following amino acid sequence (H1-B), CDRH2 is a polypeptide including the following amino acid sequence (H2-B), and CDRH3 is a polypeptide including the amino following acid sequence (H3-B). Further, as described above, the light chain variable region (4) includes CDRL1, CDRL2, and CDRL3, wherein CDRL1 is a polypeptide including the amino acid sequence (L1-A), CDRL2 is a polypeptide including the amino acid sequence (L2-A), and CDRL3 is a polypeptide including the amino acid sequence (L3-A).

(H1-B) the following amino acid sequence (H1-B1), (H1-B2), or (H1-B3):

(H1-B1) an amino acid sequence of SEQ ID NO: 4 (GYAFSTSW),

(H1-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 4, and

(H1-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 4.

(H2-B) the following amino acid sequence (H2-B1), (H2-B2), or (H2-B3):

(H2-B1) an amino acid sequence of SEQ ID NO: 5 (IYPGDGDT),

(H2-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 5, and

(H2-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 5.

(H3-B) the following amino acid sequence (H3-B1), (H3-B2), or (H3-B3):

(H3-B1) an amino acid sequence of SEQ ID NO: 6 (SNDGYYVGY),

(H3-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 6, and

(H3-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 6.

In each CDR, the “identity” is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more.

In each CDR, “one or several” relating to substitution or the like is, for example, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1.

In the combination of (2) and (4), the heavy chain variable region (2) includes a polypeptide consisting of the following amino acid sequence (H-B), for example. Further, the light chain variable region (4) includes a polypeptide consisting of the amino acid sequence (L-A), for example.

(H-B) the following amino acid sequence (H-B1), (H-B2), or (H-B3):

(H-B1) an amino acid sequence of SEQ ID NO: 14,

SEQ ID NO: 14: QVQLQQSGPELVKPGASVKISCKASGYAFSTSWMNWVKQRPGQGLEWIG RIYPGDGDTNYNGKFKGKATLTADKSSSTAYMQLSSLTSVDSAVYFCAR SNDGYYVGYWGQGTTLTVSS, (H-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 14, and (H-B3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 14.

The amino acid sequence (H-B1) is a sequence including the amino acid sequences (H1-B1) of CDRH1, (H2-B1) of CDRH2, and (H3-B1) of CDRH3, for example. The amino acid sequence (H-B2) may be an amino acid sequence including the amino acid sequences (H1-B1) of CDRH1, (H2-B1) of CDRH2, and (H3-B1) of CDRH3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 14, for example. The amino acid sequence (H-B3) may be an amino acid sequence including the amino acid sequences (H1-B1) of CDRH1, (H2-B1) of CDRH2, and (H3-B1) of CDRH3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 14, for example.

In the antibody of the present invention, for example, the heavy chain variable region is the (H-B1) and the light chain variable region is the (L-A1). The antibody of this combination is hereinafter also referred to as an “antibody 13H11”.

In the polypeptide of the heavy chain variable region and the polypeptide of the light chain variable region, the “identity” is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more, respectively.

In the polypeptide of the heavy chain variable region and the polypeptide of the light chain variable region, “one or several” relating to substitution or the like is, for example, 1 to 20, 1 to 15, 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1, respectively.

In the combination of (2) and (4), the heavy chain (2) includes, for example, a polypeptide consisting of the following amino acid sequence (HB). Further, the light chain (4) includes, for example, a polypeptide consisting of the amino acid sequence (LA).

(2) a heavy chain including a polypeptide consisting of the following amino acid sequence (HB):

(HB) the following amino acid sequence (HB1), (HB2), or (HB3):

(HB1) an amino acid sequence of SEQ ID NO: 18,

(HB2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 18, and

(HB3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 18.

The amino acid sequence (HB1) is a sequence including the amino acid sequences (H1-B1) of CDRH1, (H2-B1) of CDRH2, and (H3-B1) of CDRH3 and/or a sequence including the amino acid sequence (H-B1). The amino acid sequence (HB2) may be an amino acid sequence including the amino acid sequence (H1-B1) of CDRH1, (H2-B1) of CDRH2, and (H3-B1) of CDRH3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 18, for example. The amino acid sequence (HB2) may be an amino acid sequence including the amino acid sequence (H-B1) and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 18, for example. The amino acid sequence (HB3) may be an amino acid sequence including the amino acid sequence (H1-B1) of CDRH1, (H2-B1) of CDRH2, and (H3-B1) of CDRH3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 18, for example. The amino acid sequence (HB3) may be an amino acid sequence including the amino acid sequence (H-B1) and in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 18, for example.

In the antibody of the present invention, for example, the heavy chain is the (HB1) and the light chain is the (LA1). The antibody of this combination is hereinafter also referred to as “13H11”.

In the polypeptide of the heavy chain and the polypeptide of the light chain, the “identity” is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more, respectively.

In the polypeptide of the heavy chain and the polypeptide of the light chain, “one or several” relating to substitution or the like is, for example, 1 to 80, 1 to 60, 1 to 40, 1 to 30, 1 to 20, 1 to 15, 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1, respectively.

Combination of (3) and (4)

The antibody or the like of the combination of (3) and (4) is also referred to as, for example, an antibody 15B2 group. In the combination of (3) and (4), the heavy chain variable region (3) includes CDRH1, CDRH2, and CDRH3, wherein CDRH1 is a polypeptide including the following amino acid sequence (H1-C), CDRH2 is a polypeptide including the following amino acid sequence (H2-C), and CDRH3 is a polypeptide including the following amino acid sequence (H3-C). Further, as described above, the light chain variable region (4) includes

CDRL1, CDRL2, and CDRL3, wherein CDRL1 is a polypeptide including the amino acid sequence (L1-A), CDRL2 is a polypeptide including the amino acid sequence (L2-A), and CDRL3 is a polypeptide including the amino acid sequence (L3-A).

(H1-C) the following amino acid sequence (H1-C1), (H1-C2), or (H1-C3):

(H1-C1) an amino acid sequence of SEQ ID NO: 7 (GYTFTSYY),

(H1-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 7, and

(H1-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 7.

(H2-C) the following amino acid sequence (H2-C1), (H2-C2), or (H2-C3):

(H2-C1) an amino acid sequence of SEQ ID NO: 8 (INPSNGGT),

(H2-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 8, and

(H2-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 8.

(H3-C) the following amino acid sequence (H3-C1), (H3-C2), or (H3-C3):

(H3-C1) an amino acid sequence of SEQ ID NO: 9 (GYYGNPFFAY),

(H3-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 9, and

(H3-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 9.

In each CDR, the “identity” is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more.

In each CDR, “one or several” relating to substitution or the like is, for example, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1.

In the combination of (3) and (4), the heavy chain variable region (3) includes a polypeptide consisting of the following amino acid sequence (H-C), for example. Further, the light chain variable region (4) includes a polypeptide consisting of the amino acid sequence (L-A), for example.

(H-C) the following amino acid sequence (H-C1), (H-C2), or (H-C3):

(H-C1) an amino acid sequence of SEQ ID NO: 15,

SEQ ID NO: 15: QVQLQQSGAELVKPGASVKLSCKASGYTFTSYYMYWVKQRPGQGLEWIG EINPSNGGTNFNEKFKNKATLTVDKSSNTAYMQLNSLTSEDSAVYYCTR GYYGNPFFAYWGQGTLVTVSA, (H-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 15, and (H-C3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 15.

The amino acid sequence (H-C1) is a sequence including the amino acid sequences (H1-C1) of CDRH1, (H2-C1) of CDRH2, and (H3-C1) of CDRH3, for example. The amino acid sequence (H-C2) may be an amino acid sequence including the amino acid sequences (H1-C1) of CDRH1, (H2-C1) of CDRH2, and (H3-C1) of CDRH3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 15, for example. The amino acid sequence (H-C3) may be an amino acid sequence including the amino acid sequences (H1-C1) of CDRH1, (H2-C1) of CDRH2, and (H3-C1) of CDRH3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 15, for example.

In the antibody of the present invention, for example, the heavy chain variable region is the (H-C1) and the light chain variable region is the (L-A1). The antibody of this combination is hereinafter also referred to as an “antibody 15B2”.

In the polypeptide of the heavy chain variable region and the polypeptide of the light chain variable region, the identity is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more, respectively.

In the polypeptide of the heavy chain variable region and the polypeptide of the light chain variable region, “one or several” relating to substitution or the like is, for example, 1 to 20, 1 to 15, 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1, respectively.

In the combination of (3) and (4), the heavy chain (3) includes a polypeptide consisting of the following amino acid sequence (HC), for example. Further, the light chain (4) includes a polypeptide consisting of the amino acid sequence (LA), for example.

(3) a heavy chain including a polypeptide consisting of the following amino acid sequence (HC):

(HC) the following amino acid sequence (HC1), (HC2), or (HC3):

(HC1) an amino acid sequence of SEQ ID NO: 19,

(HC2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 19, and

(HC3) an amino acid sequence in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 19.

The amino acid sequence (HC1) is a sequence including the amino acid sequences (H1-C1) of CDRH1, (H2-C1) of CDRH2, and (H3-C1) of CDRH3, and/or a sequence including the amino acid sequence (H-C1). The amino acid sequence (HC2) may be an amino acid sequence including the amino acid sequences (H1-C1) of CDRH1, (H2-C1) of CDRH2, and (H3-C1) of CDRH3 and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 19, for example. The amino acid sequence (HC2) may be an amino acid sequence including the amino acid sequence (H-C1) and having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 19, for example. The amino acid sequence (HC3) may be an amino acid sequence including the amino acid sequences (H1-C1) of CDRH1, (H2-C1) of CDRH2, and (H3-C1) of CDRH3 and in which one or several amino acids are deleted, substituted, inserted, and/or added in the amino acid sequence of SEQ ID NO: 19, for example. The amino acid sequence (HC3) may be an amino acid sequence including the amino acid sequence (H-C1) and in which one or several amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 19, for example.

In the antibody of the present invention, for example, the heavy chain is the (HC1) and the light chain is the (LA1). The antibody of this combination is hereinafter also referred to as “15B2”.

In the polypeptide of the heavy chain and the polypeptide of the light chain, the “identity” is, for example, 80% or more, 85% or more, 90% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more, respectively.

In the polypeptide of the heavy chain and the polypeptide of the light chain, “one or several” relating to substitution or the like is, for example, 1 to 80, 1 to 60, 1 to 40, 1 to 30, 1 to 20, 1 to 15, 1 to 10, 1 to 9, 1 to 8, 1 to 7, 1 to 6, 1 to 5, 1 to 4, 1 to 3, 1 or 2, or 1, respectively.

In the present invention, the amino acid sequences of SEQ ID NOs: 1 to 20 are, for example, amino acid sequences derived from mice.

The binding between the antibody or the like of the present invention and CHIKV can be verified, for example, by a method for detecting binding between CHIKV and the antibody or the like in the description of the detection method of the present invention described below. The detection method is preferably an immunostaining method, and more preferably an indirect method. In the indirect method, for example, when the target antibody binds to CHIKV and/or when the target antibody binds to an Env protein and the signal that shows the binding thereto is strong as compared to a negative control containing no CHIKV or Env protein, the target antibody can be determined to be bound to CHIKV or an Env protein.

The antibody or the like of the present invention may further include a labeling substance, for example. The labeling substance is not particularly limited, and examples thereof include a fluorescent substance, a dye, an isotope, and an enzyme. Examples of the fluorescent substance include fluorophores such as pyrene, TAMRA, fluorescein, Cy3 dye, Cy5 dye, FAM dye, rhodamine dye, Texas red dye, JOE, MAX, HEX, TYE, and the like. Examples of the dye include Alexa dyes such as Alexa488, Alexa647 and the like.

The antibody or the like of the present invention may be immobilized on, for example, a carrier, a porous body, or the like. The carrier is not particularly limited, and examples thereof include a substrate, a bead, and a container, and examples of the container include a microplate, and a tube.

The method for producing an antibody or the like of the present invention is not particularly limited, and the antibody or the like can be produced in a genetic engineering manner based on the above-described amino acid sequence information, for example. Specifically, for example, the antibody or the like can be produced as follows. Note that the present invention is not limited to this illustration.

First, a vector containing a nucleic acid sequence encoding the amino acid sequence of each of the regions, the heavy chain, and/or the light chain in the antibody or the like of the present invention is transfected into a host to obtain a transformant. Then, the transformant is cultured, and a fraction containing an antibody that binds to the Chikungunya virus, specifically, an Env protein, is recovered, and the antibody is isolated or purified from the obtained recovered fraction.

Examples of the vector include a vector containing a nucleic acid sequence encoding the heavy chain variable region, a vector containing a nucleic acid sequence encoding the light chain variable region, a vector containing a nucleic acid sequence encoding the heavy chain, and a vector containing a nucleic acid sequence encoding the light chain. The host is not particularly limited and may be any host into which the vector can be transfected and in which the nucleic acid sequence in the vector can be expressed. Examples of the host include mammalian cells such as HEK cells, CHO cells, COS cells, NSO cells, SP2/0 cells, and the like. The method for transfecting the vector into a host is not particularly limited, and known methods can be employed.

The method for culturing the transformant is not particularly limited, and can be appropriately determined depending on the type of the host. A fraction containing the antibody can be recovered as a liquid fraction by crushing the cultured transformant, for example. Isolation or purification of the antibody is not particularly limited, and known methods can be employed.

In the present invention, the antibody is, for example, a monoclonal antibody. Examples of the monoclonal antibody include a monoclonal antibody obtained by immunizing an animal, a chimeric antibody, a humanized antibody, and a human antibody (also referred to as a fully human antibody).

The chimeric antibody is an antibody obtained by linking a variable region of an antibody derived from a non-human animal and a constant region of a human antibody. The chimeric antibody can be produced, for example, as follows. First, a gene of a variable region (V region) of a monoclonal antibody derived from a non-human animal that binds to Chikungunya virus, specifically, an Env protein, is prepared, the gene of the variable region is linked to a gene of a constant region (C region) of a human antibody, and the resultant is further linked to an expression vector. Then, the cells transfected with the expression vector are cultured, and the target chimeric antibody secreted into the culture solution is recovered, thereby preparing the chimeric antibody. The animal from which the gene of the variable region is derived is not particularly limited, and examples thereof include rats and mice. The method for producing the chimeric antibody is not limited thereto, and can be produced with reference to a known method such as a method described in JPH3(1991)-73280A, for example.

The humanized antibody is an antibody in which only the CDR is derived from a non-human animal and the other region is derived from a human. The humanized antibody can be produced, for example, as follows. First, a gene of the CDR of a monoclonal antibody from a non-human animal is prepared and transplanted (CDR-grafting) into a gene of a human antibody, e.g., a constant region, and the resultant is further linked to an expression vector. Then, by culturing the cells transfected with the expression vector, a humanized antibody transplanted with the target CDR is secreted into the culture solution. By recovering the secreted antibody, the humanized antibody can be prepared. The animal from which the CDR is derived is not particularly limited, and examples thereof include rats and mice. The method for producing a humanized antibody is not limited thereto, and can be produced with reference to known methods such as methods described in JPH4(1992)-506458A, JPS62(1987)-296890A, and the like, for example.

The human antibody is an antibody in which the entire region is of human origin. The human antibody can be produced by transfecting a human antibody gene into a non-human animal, for example. As the animal to be transfected with the human antibody gene, for example, a transgenic animal for human antibody production can be used. The type of the animal is not particularly limited, and the animal may be, for example, a mouse. As to the method for producing the human antibody, reference can be made to known methods such as methods described in, for example, Nature Genetics, Vol. 7, p. 13-21, 1994; Nature Genetics, Vol. 15, p. 146-156, 1997; JPH4(1992)-504365A; JPH7(1995)-509137A; WO94/25585; Nature, Vol. 368, p. 856-859, 1994; and JPH6(1994)-500233A. Also, the human antibody can be produced using a phage display method, for example. The human antibody can be produced with reference to a known method described in Marks, J. D. et al: J. Mol. Biol., Vol. 222, p. 581-59′7, 1991, for example.

The antibody or the like of the present invention can also be prepared by immunizing an animal with an antibody, for example. The antigen is, for example, Chikungunya virus, specifically, a protein consisting of the full-length amino acid sequence of the Env protein or a peptide fragment thereof. Preferably, the antigen is immunized multiple times. In this case, the antigen to be immunized each time is preferably Chikungunya virus or an Env protein of different genotypes, or a peptide fragment thereof, for example. The peptide fragment may be, for example, a peptide fragment consisting solely of an antigenic determinant (epitope) or a peptide fragment including the antigenic determinant.

The monoclonal antibody obtained by immunization on an animal can be produced with reference to a known method such as the method described in “Current Protocols in Molecular Biology” (John Wiley & Sons (1987)), Antibodies: A Laboratory Manual, Ed. Harlow and David Lane, Cold Spring Harbor Laboratory(1988)), for example. Specifically, for example, an animal is immunized with an antigen, and antibody-producing cells collected from the immunized animal are fused with myeloma cells lacking the ability to produce an autoantibody, thereby producing a hybridoma. Subsequently, antibody-producing cells are screened from the hybridoma to produce a single clone of hybridoma by cloning. Then, the hybridoma clone is administered to an animal, and a monoclonal antibody is purified from the obtained peritoneal cavity. Alternatively, the hybridoma is cultured, and a monoclonal antibody is purified from the culture solution thereof. Thus, by producing the hybridoma clone, a monoclonal antibody having uniform specificity can be stably supplied.

Preferably, the myeloma cells are derived from, for example, mice, rats, humans, and the like. The myeloma cells and the antibody-producing cells may be derived from the same or different species, for example, but are preferably derived from the same species.

The antibody or the like of the present invention may be, in place of the above-described antibody or the like of the present invention, an antibody against Chikungunya virus that binds to ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV and that does not bind to Sindbis virus or an anti-binding fragment of the antibody, for example. More specifically, the antibody or the like of the present invention may be, for example, an antibody or the like that binds to an Env protein of ECSA type CHIKV, an Env protein of WA type CHIKV, and an Env protein of Asian type CHIKV and that does not bind to Sindbis virus. The antibody or the like of the present invention may be, in place of the above-described antibody or the like of the present invention, an antibody that binds to ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV, that does not bind to Sindbis virus, and that competes with a reference antibody for the binding to ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV, for example, wherein the reference antibody may be the above-described antibody or the like of the present invention, i.e., the antibody 3D11 group, the antibody 13H11 group, or the antibody 15B2 group, the antibody 3D11, the antibody 13H11, or the antibody 15B2, or 3D11, 13H11, or 15B2. The antibody or the like of the present invention may be, in place of the above-described antibody or the like of the present invention, an antibody that binds to an Env protein of ECSA type CHIKV, an Env protein of WA type CHIKV, and an Env protein of Asian type CHIKV, that does not bind to Sindbis virus, and that competes with a reference antibody for the binding to an Env protein of ECSA type CHIKV, an Env protein of WA type CHIKV, and an Env protein of Asian type CHIKV, for example, wherein the reference antibody may be the above-described antibody or the like of the present invention, i.e., the antibody 3D11 group, the antibody 13H11 group, or the antibody 15B2 group, the antibody 3D11, the antibody 13H11 or the antibody 15B2, or 3D11, 13H11 or 15B2. The Env protein of ECSA type CHIKV may be, for example, a protein consisting of the amino acid sequence of SEQ ID NO: 21. The Env protein of WA type CHIKV may be, for example, a protein consisting of the amino acid sequence of SEQ ID NO: 22. The Env protein of Asian type CHIKV may be, for example, a protein consisting of the amino acid sequence of SEQ ID NO: 23. The SINV may be, for example, the strain R68 to be described below.

Gene, Expression Vector, and Transformant

The coding gene of the present invention is a coding gene for an antibody against Chikungunya virus or an antigen-binding fragment of the antibody, and includes a polynucleotide encoding the amino acid sequence of the antibody or the antigen-binding fragment of the present invention.

By expressing the coding gene of the present invention, the antibody or the like of the present invention can be obtained. The sequence of the coding gene of the present invention is not particularly limited, and any sequence may be used as long as it encodes the amino acid sequence of the antibody or the like of the present invention, and may be a sense sequence or an antisense sequence.

The expression vector of the present invention is an expression vector of an antibody against Chikungunya virus or an antigen-binding fragment of the antibody, and includes the coding gene of the present invention. In the expression vector, the coding gene is linked to the linking vector in such a manner to be capable of expressing the antibody or the antigen-binding fragment of the antibody of the invention. The expression vector of the present invention may be any vector as long as it is capable of expressing the antibody or the like of the present invention, and other configurations are not particularly limited.

The expression vector of the present invention may be, for example, an expression vector including a nucleic acid sequence encoding the heavy chain variable region and a nucleic acid sequence encoding the light chain variable region, or may be a set of an expression vector including a nucleic acid sequence encoding the heavy chain variable region and an expression vector including a nucleic acid sequence encoding the light chain variable region. The expression vector of the present invention can be prepared, for example, by linking the coding gene of the invention to a linking vector. The type of the linking vector linking to the coding gene is not particularly limited, and may be, for example, pUC. The linking vector may be appropriately set, for example, depending on a host into which the expression vector is transfected. The host is not particularly limited, and examples thereof include mammalian cells such as CHO cells.

The transformant of the present invention is a transformant expressing the antibody or the like of the present invention, and includes a host and the coding gene of the present invention. The transformant of the present invention may include the coding gene of the present invention in such a manner to be capable of expressing. Preferably, the transformant includes the expression vector of the present invention, for example. The method for transfecting the expression vector into the host is not particularly limited, and known methods can be employed.

Detection Kit

The detection kit for Chikungunya virus of the present invention includes the antibody or the antigen-binding fragment of the antibody of the present invention, as described above. The detection kit of the present invention is characterized in that it includes the antibody or the like of the present invention, and other configurations and conditions are not particularly limited. According to the kit of the present invention, for example, the detection method of the present invention described below can be conveniently performed. Regarding the detection kit of the present invention, for example, reference can be made to the description as to the antibody or the like of the present invention.

The detection kit of the present invention may further include, for example, a detection substance that detects binding between CHIKV and the antibody or the like of the present invention, more specifically, binding between the Env protein and the antibody or the like of the invention, for example. The detection substance may be, for example, a combination of a detectable labeled antibody to the antibody or the like and a substrate or the like to the label.

The detection kit of the present invention may include other components in addition to the antibody or the like of the present invention, for example. Such components include, for example, the carriers, buffers, instructions for use, and the like.

In the detection kit of the present invention, for example, the antibody or the like and other components such as the buffer may be contained in separate containers or may be contained in the same container in a mixed or unmixed manner. When the antibody or the like and the other components are mixed and contained in the same container, the detection kit of the present invention can also be referred to as a detection reagent.

Detection Method

The method for detecting Chikungunya virus of the present invention, includes: a detection step of bringing a sample into contact with the antibody or the antigen-binding fragment of the antibody according to the present invention to bind Chikungunya virus in the sample to the antibody or the antigen-binding fragment of the antibody, thereby detecting Chikungunya virus in the sample. The detection method of the present invention is characterized in that the antibody or the antigen-binding fragment of the antibody of the present invention is used, and other steps and conditions are not particularly limited. Regarding the detection method of the present invention, reference can be made to the description as to the antibody, detection kit, or the like of the present invention.

The detection method of the present invention uses the antibody or the like of the present invention. The antibody or the like binds to ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV, and more specifically binds to an Env protein of ECSA type CHIKV, an Env protein of WA type CHIKV, and an Env protein of Asian type CHIKV, for example. Thus, the detection method of the present invention can indirectly detect CHIKV by detecting an Env protein of CHIKV, for example. According to the detection method of the present invention, any of the ECSA type CHIKV, the WA type CHIKV, and the Asian type CHIKV can be detected. The antibody or the like does not bind to Sindbis virus, for example. Thus, the detection method of the present invention can reduce the possibility of erroneously detecting a sample containing a SINV as including a CHIKV as compared to a case of using a CK119 antibody, for example. Further, the antibody or the like of the present invention binds to an Env protein, for example. Thus, the detection method of the present invention can also be referred to as a method for detecting an Env protein.

According to the detection method of the present invention, it is possible to analyze the presence or absence of CHIKV or the amount of CHIKV in a sample. Thus, the detection method of the present invention can also be referred to as an analysis method, for example.

In the detection method of the present invention, the origin of the sample is not particularly limited, and examples thereof include humans and non-human animals, and examples of the non-human animals include mammals such as a mouse, a rat, a dog, a monkey, a rabbit, a sheep, a horse, and the like as described above.

The type of the sample is not particularly limited, and examples thereof include biological samples such as body fluids, urine, body fluid-derived cells, organs, tissues, and cells separated from a living body. Examples of the body fluid include body cavity fluid such as blood, synovial fluid, and the like, lymph, and tissue fluid, and specific examples thereof include whole blood, serum, and plasma. The biological sample is preferably whole blood, serum, or plasma, and more preferably serum or plasma. For example, as to the sample, the collected sample may be used as it is in the detection method of the present invention, or may be used after performing other treatment such as dilution with a liquid or the like. The liquid is not particularly limited, and examples thereof include water, physiological saline, a buffer, and a medium. In addition, the sample may be subjected to an acid treatment in advance, for example. Thereby, in the detection method of the present invention, for example, the antibody and the Chikungunya virus can be dissociated when the Chikungunya virus in the sample and the antibody form an antigen-antibody complex, so that the Chikungunya virus can be detected with more sensitivity. The acid used in the acid treatment is not particularly limited, and examples thereof include hydrochloric acid and acetic acid.

The sample may be, for example, a sample containing CHIKV, a sample containing no CHIKV, or a sample which is unknown whether it contains CHIKV or not.

The sample may be, for example, a liquid sample or a solid sample. In the case of the solid sample, for example, it is preferable to mix with the liquid and use it as a liquid sample because in that way the sample can easily be contact with the antibody or the like and is easy to handle.

The detection step includes, for example, a contact step of bringing the sample into contact with the antibody or the like to bind CHIKV in the sample to the antibody or the like, and a binding detection step of detecting binding between CHIKV and the antibody or the like. Also, the detection step further includes a step of analyzing the presence or absence of CHIKV or the amount of CHIKV in the sample based on the result of the binding detection step.

In the contact step, a method for bringing the sample into contact with the antibody or the like is not particularly limited. The contact between the sample and the antibody or the like is preferably performed in a liquid, for example. The liquid is not particularly limited, and examples thereof include water, physiological saline, and a buffer.

In the contact step, the contact conditions between the sample and the antibody or the like are not particularly limited. The contact temperature is, for example, 4° C. to 37° C. The contact time is, for example, 10 to 120 minutes. The concentration of the antibody or the like in the mixture of the sample and the antibody or the like is not particularly limited, and is, for example, 0.1 m/ml to 1 mg/ml.

In the contact step, the antibody or the like may be, for example, an immobilized antibody or the like which is immobilized on a carrier, or an unimmobilized free antibody or the like. In the latter case, the antibody or the like is brought into contacted with the sample in a container, for example. The antibody or the like is preferably the immobilized antibody or the like because it is excellent in handleability, for example. The carrier is not particularly limited, and examples thereof include substrates, beads, and containers, and examples of the container include microplates and tubes.

The binding detection step is a step of detecting binding between CHIKV in the sample and the antibody or the like, as described above. By detecting whether or not there is binding therebetween, for example, the presence or absence of CHIKV in the sample can be analyzed (qualitative analysis can be performed), and by detecting the degree (binding amount) of binding therebetween, for example, the amount of CHIKV in the sample can be analyzed (quantitative analysis can be performed).

Then, when the binding between CHIKV and the antibody or the like cannot be detected, it can be determined that the sample contains no CHIKV, and when the binding is detected, it can be determined that the sample contains CHIKV. In addition, it is also possible to obtain the relationship between the number of CHIKV and the binding amount in advance, and to analyze the amount of CHIKV in the sample from the binding amount based on the relationship.

The method for detecting the binding between CHIKV and the antibody or the like is not particularly limited, and for example, a known method of utilizing binding between an antibody or an antigen-binding fragment and an antigen can be employed. Specific examples of the detection method include an immunoantibody method, an immunostaining method, an ELISA method, a flow cytometry, and a Western blotting method.

When the sample is a biological sample derived from a subject, for example, the detection method of the present invention may include a test step of testing a risk of CHIKV infection of the subject by comparing the amount of CHIKV in a biological sample of the subject (hereinafter, also referred to as a subject biological sample) with a reference value. In this case, the detection method of the present invention can also be referred to as, for example, a method for testing the risk of CHIKV infection. The reference value is not particularly limited, and may be, for example, the amount of CHIKV in a healthy subject, a CHIKV infected subject, or the like. In the case of prognostic assessment, the reference value may be, for example, the amount of CHIKV after treatment of the same subject.

The reference value can be obtained, for example, using a biological sample isolated from a healthy subject and/or an infected subject (hereinafter, also referred to as a “reference biological sample”) as described above. The reference value may be measured simultaneously with, for example, a subject biological sample of the subject, or may be measured in advance. The latter case is preferable because it is unnecessary to obtain a reference value every time the subject biological sample of the subject is measured, for example. It is preferable that the subject biological sample of the subject and the reference biological sample be collected under the same conditions, for example, and the detection (e.g., quantitative analysis) of CHIKV is performed under the same conditions.

In the test step, a method for assessing the risk of CHIKV infection of a subject is not particularly limited, and can be appropriately determined according to the type of the reference value. Specifically, when the amount of CHIKV in the subject biological sample of the subject is significantly higher than the amount of CHIKV in the reference biological sample of the healthy subject, when the amount of CHIKV in the subject biological sample of the subject is the same as the amount of CHIKV in the reference biological sample of the infected subject (when there is no significant difference therebetween), and/or when the amount of CHIKV in the subject biological sample of the subject is significantly higher than the amount of CHIKV in the reference biological sample of the infected subject, the subject can be assessed as at risk or at high risk of CHIKV infection. On the other hand, when the amount of CHIKV in the subject biological sample of the subject is the same as the amount of CHIKV in the reference biological sample of the healthy subject (when there is no significant difference therebetween), when the amount of CHIKV in the subject biological sample of the subject is significantly lower than the amount of CHIKV in the reference biological sample of the healthy subject, and/or when the amount of CHIKV in the subject biological sample of the subject is significantly lower than the amount of CHIKV in the reference biological sample of the infected subject, the subject can be assessed as having no risk or a low risk of CHIKV infection.

In the test step, in the case of prognostic assessment, for example, the assessment can be made in the same manner as described above or by using the amount of CHIKV in a reference biological sample after treatment of the same subject as a reference value. As a specific example, when the amount of CHIKV in the subject biological sample of the subject is significantly higher than the reference value, the subject can be assessed as at risk of relapse or deterioration (becoming severe) after the treatment. Also, when the amount of CHIKV in the subject biological sample of the subject is the same as the reference value (when there is no significant difference therebetween) and/or when the amount of CHIKV in the subject biological sample of the subject is significantly lower than the reference value, the subject can be assessed as having no risk or a low risk of relapse after the treatment.

In the present invention, for example, biological samples of the same subject may be collected over time, and the amounts of CHIKV in the biological samples may be compared. Thereby, for example, it is possible to judge that the possibility of becoming severe increases if the expression level increases over time, and it is possible to judge that the possibility of becoming severe decreases or that the subject has healed if the expression level decreases over time.

Diagnostic Method and Diagnostic Kit for Chikungunya Virus

The diagnostic method for Chikungunya virus of the present invention includes a detection step of bringing a sample into contact with the antibody or the antigen-binding fragment of the antibody of the present invention to bind Chikungunya virus in the sample to the antibody or the antigen-binding fragment of the antibody, thereby detecting Chikungunya virus in the sample. Further, the diagnostic kit for Chikungunya virus of the present invention includes the antibody or the antigen-binding fragment of the antibody of the present invention. Regarding the diagnostic method and the diagnostic kit, reference can be made to the description as to the antibody or the like, the detection kit, the detection method, and the like of the present invention.

EXAMPLES

The examples of the present invention are described below. The present invention, however, is not limited by the following examples. Commercially available reagents were used based on their protocols unless otherwise indicated.

Example 1

The anti CHIKV antibody of the present invention was produced. General methods were employed unless otherwise indicated.

As antigens, cultured cells infected with ECSA type CHIKV and Sendai virus expressing 6K-E1 protein of Asian type CHIKV were used. Specifically, mice (Balb/c) aged 4 to 6 weeks were immunized with a mixture of the cultured cells and CFA (Complete Freund's adjuvant) for the first time. Two weeks after the first immunization, the mice were immunized with a mixture of the cultured cells and IFA (Incomplete Freund's adjuvant) for the second time. Two weeks after the second immunization, the mice were immunized with a mixture of the virus and IFA for the third time. Three days after the third immunization, B cells were prepared from the mice and hybridomas were prepared from the B cells by a conventional method. The resulting hybridomas were screened for anti CHIKV antibody-producing hybridomas using their culture solution.

Consequently, three hybridomas (3D11, 13H11, and 15B2 strains) were isolated. Three monoclonal antibodies (3D11, 13H11, and 15B2) were obtained as anti CHIKV antibodies generated from these hybridomas. The isotypes of 3D11, 13H11, and 15B2 were IgG2aκ, IgG1κ, and IgG2bκ, respectively.

Amino acid sequences were determined for the anti CHIKV antibodies 3D11, 13H11, and 15B2. The results thereof are shown below. The light chains 3D11, 13H11, and 15B2 all have the same amino acid sequence. In each amino acid sequence, the underlined amino acid sequences correspond to the amino acid sequences of CDR1, CDR2 and CDR3, respectively, from the N-terminus toward the C-terminus. In addition, in each amino acid sequence, an amino acid sequence enclosed in parentheses corresponds to an amino acid sequence of a variable region.

3D11 heavy chain (SEQ ID NO: 17) [QVQLQQSGAELARPGASVKLSCKASGYTFTSYWMQWVKQRPGQGLEWI GAIYPGDGDTRYTQKFKGKATLTADKSSSTAYMQLSSLASEDSAVYYCA RSYDPFDYWGQGTTLTVSS]AKTTAPSVYPLAPVCGDTTGSSVTLGCLV KGYFPEPVTLTWNSGSLSSGVHTFPAVLQSDLYTLSSSVTVTSSTWPSQ SITCNVAHPASSTKVDKKIEPRGPTIKPCPPCKCPAPNLLGGPSVFIFP PKIKDVLMISLSPIVTCVVVDVSEDDPDVQISWFVNNVEVHTAQTQTHR EDYNSTLRVVSALPIQHQDWMSGKEFKCKVNNKDLPAPIERTISKPKGS VRAPQVYVLPPPEEEMTKKQVTLTCMVTDFMPEDIYVEWTNNGKTELNY KNTEPVLDSDGSYFMYSKLRVEKKNWVERNSYSCSVVHEGLHNHEITTK SFSRTPGK 13H11 heavy chain (SEQ ID NO: 18) [QVQLQQSGPELVKPGASVKISCKASGYAFSTSWMNWVKQRPGQGLEWI GRIYPGDGDTNYNGKFKGKATLTADKSSSTAYMQLSSLTSVDSAVYFCA RSNDGYYVGYWGQGTTLTVSS]AKTTPPSVYPLAPGSAAQTNSMVTLGC LVKGYFPEPVTVTWNSGSLSSGVHTFPAVLQSDLYTLSSSVTVPSSTWP SETVTCNVAHPASSTKVDKKIVPRDCGCKPCICTVPEVSSVFIFPPKPK DVLTITLTPKVTCVVVDISKDDPEVQFSWFVDDVEVHTAQTQPREEQFN STFRSVSELPIMHQDWLNGKEFKCRVNSAAFPAPIEKTISKTKGRPKAP QVYTIPPPKEQMAKDKVSLTCMITDFFPEDITVEWQWNGQPAENYKNTQ PIMDTDGSYFVYSKLNVQKSNWEAGNTFTCSVLHEGLHNHHTEKSLSHS PGK 15B2 heavy chain (SEQ ID NO: 19) [QVQLQQSGAELVKPGASVKLSCKASGYTFTSYYMYWVKQRPGQGLEWI GEINPSNGGTNFNEKFKNKATLTVDKSSNTAYMQLNSLTSEDSAVYYCT RGYYGNPFFAYWGQGTLVTVSA]AKTTPPSVYPLAPGCGDTTGSSVTLG CLVKGYFPESVTVTWNSGSLSSSVHTFPALLQSGLYTMSSSVTVPSSTW PSQTVTCSVAHPASSTTVDKKLEPSGPISTINPCPPCKECHKCPAPNLE GGPSVFIFPPNIKDVLMISLTPKVTCVVVDVSEDDPDVQISWFVNNVEV HTAQTQTHREDYNSTIRVVSTLPIQHQDWMSGKEFKCKVNNKDLPSPIE RTISKIKGLVRAPQVYILPPPAEQLSRKDVSLTCLVVGFNPGDISVEWT SNGHTEENYKDTAPVLDSDGSYFIYSKLNMKTSKWEKTDSFSCNVRHEG LKNYYLKKTISRSPGK 3D11, 13H11, and 15B2 light chain (SEQ ID NO: 20) [NIVMTQSPKSMSMSVGERVTLTCKASENVVTYVSWYQQKPEQSPKLLI YGASNRYTGVPDRFTGSGSATDFTLTISSVQAEDLADYHCGQGYSYPYT FGGGTKLEI]KRADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPKDIN VKWKIDGSERQNGVLNSWTDQDSKDSTYSMSSTLTLTKDEYERHNSYTC EATHKTSTSPIVKSFNRNEC

In the following examples, the hybridoma was administered to a mouse peritoneal cavity, and an antibody purified from the obtained ascites fluid was used as an antibody sample.

Example 2

It was examined that the antibody of the present invention binds to an Env protein of CHIKV of each genotype by indirect immunofluorescence assays (immunostaining method).

(1) Vector Preparation

Expression vectors containing an Env protein of CHIKV or a capsid protein of CHIKV were prepared in the following manner. Specifically, a codon-optimized cDNA was prepared for each cDNA encoding a capsid protein of CHIKV, or an Env protein of ECSA type (CP10 strain), WA type (37997 strain), or Asian type (CK12-686 strain). Regarding cDNA encoding the Env protein, reference was made to the nucleic acid sequence information registered in NCBI. Specifically, regarding the Env protein of ECSA type (CP10 strain), reference was made to the nucleic acid sequence information registered in NCBI Accession NO.: AB857761.1. Regarding the Env protein of WA type (37997 strain), reference was made to the genomic information registered with NCBI Accession NO.: AY726732. Regarding the Env protein of Asian type (CK12-686 strain), reference was made to the genomic information registered in NCBI Accession No.: CWIH01000001.1. A cDNA cassette encoding a capsid protein of CHIKV or an Env protein of CHIKV were transfected into pCAGGS MSII plasmid. An expression vector containing a mutant Env protein (E350D) or a mutant Env protein (D350E) was produced using an overlap primer. In the Env protein of CP10 strain, glutamic acid (E) was substituted with aspartic acid (D). In the Env proteins of CK12-686 strain and 37997 strain, aspartic acid (D) was substituted with glutamic acid (E).

(2) Preparation of Env Protein Expressing Cells

HEK293T cells were seeded in 96 well plates so as to achieve a density of 2×10⁴ cells/100 μl/well. The culture solution was a DMEM medium (manufactured by Dulbecco's Modified Eagle Medium, Life technologies) containing 10% (v/v) heat-inactivated fetal bovine serum (FBS, manufactured by Life Technologies). Culture conditions were 37° C. and 5% CO₂ (hereinafter, the same applies). At 20 hours of the seeding, the expression vector and transfection reagent (Lipofectamine® 2000, manufactured by Invitrogen Co., Ltd.) were used and transfected into HEK293T cells according to the attached protocol.

(3) Indirect Immunofluorescence Assays

Forty-eight hours after the transfection, cells in each well were immobilized using a phosphate buffer (PBS) with 3.7% (v/v) formaldehyde and then subjected to permeabilization using 1% Triton® X-100. Purified 3D11, 13H11, or 15B2 was added as a primary antibody to obtain 50 μl of supernatant or 2 μg/ml solution and the resultant was incubated for 1 hour at 37° C.

After the incubation, each well was washed with PBS and 50 μl of secondary antibody was added. The secondary antibody was an Alexa Flour 488-labeled goat anti-mouse IgG antibody (manufactured by Invitrogen). After the addition, the resultant was incubated at 37° C. for 45 minutes. Next, each well was washed with PBS, and each well was observed using a fluorescent microscope (IX71, manufactured by Olympus Co., Ltd.). The results of cells expressing the Env protein are shown in FIGS. 1A to 1C.

FIGS. 1A to 1C show photographs showing the staining results of cells expressing Env protein. FIG. 1A shows the staining results of 3D11, FIG. 1B shows the staining results of 13H11, and FIG. 1C shows the staining results of 15B2. In FIGS. 1A to 1C, the photographs show the results of cells expressing (1) Env protein of ECSA type, (2) mutant Env protein of ECSA type E350D, (3) Env protein of WA type, (4) mutant Env protein of WA type D350E, (5) Env protein of Asian type, and (6) mutant Env protein of Asian type D350E from the left column to the right column. Arrows in FIGS. 1A to 1C indicate examples of cells each stained with each antibody. In FIGS. A to 1C, as indicated by the arrows, 3D11, 13H11, and 15B2 were found to bind to any of the Env proteins. These results show that the antibody or the like of the present invention can be used for detecting three genotypes of CHIKV, more specifically, Env proteins of three genotypes of CHIKV. Although it is not shown, none of the antibodies stained the vector non-transfected cells and cells expressing the capsid protein.

In addition, as to cells expressing Env protein, when the results of staining with CK47 antibody or CK119 antibody and the results of staining with 3D11, 13H11, and 15B2 were compared, 3D11, 13H11, and 15B2 stained strongly the intracytoplasmic regions in addition to the cell surface as in the case of CK47 antibody or CK119 antibody, although it is not shown. This was presumed by the fact that, unlike CK47 antibody or CK119 antibody, 3D11, 13H11, and 15B2 also bind to the Env protein misfolding protein. This presumption does not limit the present invention in any way.

Example 3

It was examined whether the antibody of the present invention does not bind to SINV by indirect immunofluorescence assays (immunostaining method).

(1) Preparation of SINV-Infected Cells

Baby Hamster Kidney fibroblast cell line (BHK) cells were seeded in 96 well plates so as to achieve a density of 2×10⁴ cells/100 μl/well. SINV (R68 strain, obtained from Professor Kohji Morishi of Yamanashi University) was immunized with BHK cells at MOI 0.01 to prepare SINV-infected cells. BHK cells were cultured in a DMEM medium containing 10% (v/v) heat-inactivated FBS when it was not infected with SINV. BHK cells were cultured in a DMEM medium containing 2% (v/v) heat-inactivated FBS after being infected with SINV.

(2) Indirect Immunofluorescence Assays

SINV-infected cells were stained in the same manner as in Example 2(3) except that SINV-infected cells were used instead of cells after transfection, and each well was observed using the fluorescent microscope. The results are shown in FIGS. 2A to 2D.

FIGS. 2A to 2D show photographs showing the staining results of SINV-infected cells. FIG. 2A shows the staining result of 3D11, FIG. 2B shows the staining result of 13H11, FIG. 2C shows the staining result of 15B2, and FIG. 2D shows the staining result of CK119 antibody. As shown in FIG. 2D, CK119 antibody stained SINV-infected cells and showed cross-reactivity with SINV. In contrast, as shown in FIGS. 2A to 2C, 3D11, 13H11, and 15B2 did not stain SINV-infected cells and showed no cross-reactivity with SINV. These results show that the antibody or the like of the present invention does not bind to SINV.

While the present invention has been described above with reference to illustrative embodiments, the present invention is by no means limited thereto. Various changes and variations that may become apparent to those skilled in the art may be made in the configuration and specifics of the present invention without departing from the scope of the present invention.

This application claims priority from Japanese Patent Application No. 2018-022084 filed on Feb. 9, 2018. The entire subject matter of the Japanese Patent Application is incorporated herein by reference.

INDUSTRIAL APPLICABILITY

As described above, the antibody or the like of the present invention binds to three genotypes of CHIKV, namely ECSA type CHIKV, WA type CHIKV, and Asian type CHIKV. Thus, according to the antibody or the like of the present invention, for example, CHIKV can be detected regardless of the genotype, and therefore, it can be suitably used for a detection kit for CHIKV. Therefore, the present invention is extremely useful in the field of clinical testing and the like.

SEQUENCE LISTING

..¥Sequence List/Drawings¥TF18002WO_Sequence Listing_ST25.txt 

The invention claimed is:
 1. An antibody against Chikungunya virus or an antigen-binding fragment of the antibody, comprising the following heavy chain variable region (1), (2), or (3) and the following light chain variable region (4): (1) a heavy chain variable region comprising heavy chain complementarity determining regions (CDRHA)-1, CDRHA-2, and CDRHA-3: CDRHA-1 is a polypeptide comprising the following amino acid sequence (H1-A1), CDRHA-2 is a polypeptide comprising the following amino acid sequence (H2-A1), and CDRHA-3 is a polypeptide comprising the following amino acid sequence (H3-A1): (H1-A1) an amino acid sequence of SEQ ID NO: 1 (GYTFTSYW), (H2-A1) an amino acid sequence of SEQ ID NO: 2 (IYPGDGDTRYT), and (H3-A1) an amino acid sequence of SEQ ID NO: 3 (SYDPFDY), (2) a heavy chain variable region comprising CDRHB-1, CDRHB-2, and CDRHB-3: CDRHB-1 is a polypeptide comprising the following amino acid sequence (H1-B1), CDRHB-2 is a polypeptide comprising the following amino acid sequence (H2-B1), and CDRHB-3 is a polypeptide comprising the following amino acid sequence (H3-B1): (H1-B1) an amino acid sequence of SEQ ID NO: 4 (GYAFSTSW), (H2-B1) an amino acid sequence of SEQ ID NO: 5 (IYPGDGDT), and (H3-B1) an amino acid sequence of SEQ ID NO: 6 (SNDGYYVGY), (3) a heavy chain variable region comprising CDRHC-1, CDRHC-2, and CDRHC-3: CDRHC-1 is a polypeptide comprising the following amino acid sequence (H1-C1), CDRHC-2 is a polypeptide comprising the following amino acid sequence (H2-C1), and CDRHC-3 is a polypeptide comprising the following amino acid sequence (H3-C1): (H1-C1) an amino acid sequence of SEQ ID NO: 7 (GYTFTSYY), (H2-C1) an amino acid sequence of SEQ ID NO: 8 (INPSNGGT), and (H3-C1) an amino acid sequence of SEQ ID NO: 9 (GYYGNPFFAY), (4) a light chain variable region comprising light chain complementarity determining regions (CDRL)-1, CDRL-2, and CDRL-3: CDRL-1 is a polypeptide comprising the following amino acid sequence (L1-A1), CDRL-2 is a polypeptide comprising the following amino acid sequence (L2-A1), and CDRL-3 is a polypeptide comprising the following amino acid sequence (L3-A1): (L1-A1) an amino acid sequence of SEQ ID NO: 10 (ENVVTY), (L2-A1) an amino acid sequence of SEQ ID NO: 11 (GAS), and (L3-A1) an amino acid sequence of SEQ ID NO: 12 (GQGYSYPYT).
 2. An antibody against Chikungunya virus or an antigen-binding fragment of the antibody, comprising the following heavy chain variable region (1), (2), or (3) and the following light chain variable region (4): (1) a heavy chain variable region comprising a polypeptide consisting of the following amino acid sequence (H-A) that is selected from the group consisting of amino acid sequences (H-A1), (H-A2), and (H-A3): (H-A1) an amino acid sequence of SEQ ID NO: 13, (H-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 13, and (H-A3) an amino acid sequence in which one to twenty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 13, wherein each of (H-A1), (H-A2), and (H-A3) comprises sequences of heavy chain complementarity determining regions (CDRHA)-1 comprising an amino acid sequence of SEQ ID NO: 1, CDRHA-2 comprising an amino acid sequence of SEQ ID NO: 2, and CDRHA-3 comprising an amino acid sequence of SEQ ID NO: 3, wherein the CDRHA-1, the CDRHA-2, and the CDRHA-3 sequences are invariant, (2) a heavy chain variable region comprising a polypeptide consisting of the following amino acid sequence (H-B) that is selected from the group consisting of amino acid sequences (H-B1), (H-B2), and (H-B3): (H-B1) an amino acid sequence of SEQ ID NO: 14, (H-B2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 14, and (H-B3) an amino acid sequence in which one to twenty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 14, wherein each of (H-B1), (H-B2), and (H-B3) comprises sequences of CDRHB-1 comprising an amino acid sequence of SEQ ID NO: 4, CDRHB-2 comprising an amino acid sequence of SEQ ID NO: 5, and CDRHB-3 comprising an amino acid sequence of SEQ ID NO: 6, wherein the CDRHB-1, the CDRHB-2, and the CDRHB-3 sequences are invariant, (3) a heavy chain variable region comprising a polypeptide consisting of the following amino acid sequence (H-C) that is selected from the group consisting of amino acid sequences (H-C1), (H-C2), and (H-C3): (H-C1) an amino acid sequence of SEQ ID NO: 15, (H-C2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 15, and (H-C3) an amino acid sequence in which one to twenty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 15, wherein each of (H-C1), (H-C2), and (H-C3) comprises sequences of CDRHC-1 comprising an amino acid sequence of SEQ ID NO: 7, CDRHC-2 comprising an amino acid sequence of SEQ ID NO: 8, and CDRHC-3 comprising an amino acid sequence of SEQ ID NO: 9, wherein the CDRHC-1, the CDRHC-2, and the CDRHC-3 sequences are invariant, (4) a light chain variable region comprising a polypeptide consisting of the following amino acid sequence (L-A) that is selected from the group consisting of amino acid sequences (L-A1), (L-A2), and (L-A3): (L-A1) an amino acid sequence of SEQ ID NO: 16, (L-A2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 16, and (L-A3) an amino acid sequence in which one to twenty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 16, wherein each of (L-A1), (L-A2), and (L-A3) comprises sequences of light chain complementarity determining regions (CDRL)-1 comprising an amino acid sequence of SEQ ID NO: 10, CDRL-2 comprising an amino acid sequence of SEQ ID NO: 11, and CDRL-3 comprising an amino acid sequence of SEQ ID NO: 12, wherein the CDRL-1, the CDRL-2, and the CDRL-3 sequences are invariant.
 3. An antibody against Chikungunya virus or an antigen-binding fragment of the antibody, comprising the following heavy chain (1), (2), or (3) and the following light chain (4): (1) a heavy chain comprising a polypeptide consisting of the following amino acid sequence (HA) that is selected from the group consisting of amino acid sequences (HA1), (HA2), and (HA3): (HA1) an amino acid sequence of SEQ ID NO: 17, (HA2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 17, and (HA3) an amino acid sequence in which one to eighty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 17, wherein the SEQ ID NO: 17 comprises sequences of heavy chain complementarity determining regions (CDRHA)-1 comprising an amino acid sequence of SEQ ID NO: 1, CDRHA-2 comprising an amino acid sequence of SEQ ID NO: 2, and CDRHA-3 comprising an amino acid sequence of SEQ ID NO: 3, wherein the CDRHA-1, the CDRHA-2, and the CDRHA-3 sequences are invariant, (2) a heavy chain comprising a polypeptide consisting of the following amino acid sequence (HB) that is selected from the group consisting of amino acid sequences (HB1), (HB2), and (HB3): (HB1) an amino acid sequence of SEQ ID NO: 18, (HB2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 18, and (HB3) an amino acid sequence in which one to eighty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 18, wherein the SEQ ID NO: 18 comprises sequences of CDRHB-1 comprising an amino acid sequence of SEQ ID NO: 4, CDRHB-2 comprising an amino acid sequence of SEQ ID NO: 5, and CDRHB-3 comprising an amino acid sequence of SEQ ID NO: 6, wherein the CDRHB-1, the CDRHB-2, and the CDRHB-3 sequences are invariant, (3) a heavy chain comprising a polypeptide consisting of the following amino acid sequence (HC) that is selected from the group consisting of amino acid sequences (HC1), (HC2), and (HC3): (HC1) an amino acid sequence of SEQ ID NO: 19, (HC2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 19, and (HC3) an amino acid sequence in which one to eighty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 19, wherein the SEQ ID NO: 19 comprises sequences of CDRHC-1 comprising an amino acid sequence of SEQ ID NO: 7, CDRHC-2 comprising an amino acid sequence of SEQ ID NO: 8, and CDRHC-3 comprising an amino acid sequence of SEQ ID NO: 9, wherein the CDRHC-1, the CDRHC-2, and the CDRHC-3 sequences are invariant, (4) a light chain comprising a polypeptide consisting of the following amino acid sequence (LA) that is selected from the group consisting of amino acid sequences (LA1), (LA2), and (LA3): (LA1) an amino acid sequence of SEQ ID NO: 20, (LA2) an amino acid sequence having 80% or more identity with respect to the amino acid sequence of SEQ ID NO: 20, and (LA3) an amino acid sequence in which one to forty amino acids are deleted, substituted, inserted and/or added in the amino acid sequence of SEQ ID NO: 20, wherein SEQ ID NO: 20 comprises sequences of light chain complementarity determining regions (CDRL)-1 comprising an amino acid sequence of SEQ ID NO: 10, CDRL-2 comprising an amino acid sequence of SEQ ID NO: 11, and CDRL-3 comprising an amino acid sequence of SEQ ID NO: 12, wherein the CDRL-1, the CDRL-2, and the CDRL-3 sequences are invariant.
 4. The antibody against Chikungunya virus or the antigen-binding fragment of the antibody according to claim 1, wherein the antibody binds to an envelope glycoprotein of the Chikungunya virus.
 5. A detection kit for Chikungunya virus, comprising: the antibody or the antigen-binding fragment of the antibody according to claim
 1. 6. The detection kit according to claim 5, comprising: a detection reagent that detects binding between Chikungunya virus and the antibody or the antigen-binding fragment of the antibody. 